106401-57-4

Basic information

• Product Name: 2-O-BENZYL-3-O-ALLYL-SN-GLYCEROL
• Synonyms: 2-O-BENZYL-3-O-ALLYL-SN-GLYCEROL
• CAS NO: 106401-57-4
• Molecular Formula: C₁₃H₁₈O₃
• Molecular Weight: 222.28
• Mol File: 106401-57-4.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 344.4±32.0 °C(Predicted)
• Appearance: /
• Density: 1.056±0.06 g/cm3(Predicted)
• Storage Temp.: -15°C
• PKA: 14.23±0.10(Predicted)
• CAS DataBase Reference: 2-O-BENZYL-3-O-ALLYL-SN-GLYCEROL(CAS DataBase Reference)
• NIST Chemistry Reference: 2-O-BENZYL-3-O-ALLYL-SN-GLYCEROL(106401-57-4)
• EPA Substance Registry System: 2-O-BENZYL-3-O-ALLYL-SN-GLYCEROL(106401-57-4)

Safety Data

• Hazardous Substances Data: 106401-57-4(Hazardous Substances Data)

Usage

Description

2-O-Benzyl-3-O-allyl-sn-glycerol is a synthetic compound derived from glycerol, a simple polyol compound. It is characterized by the presence of a benzyl group at the 2nd carbon and an allyl group at the 3rd carbon. 2-O-BENZYL-3-O-ALLYL-SN-GLYCEROL serves as a versatile intermediate in the synthesis of various complex molecules and has potential applications in different industries.

Uses

Used in Pharmaceutical Industry:
2-O-Benzyl-3-O-allyl-sn-glycerol is used as a synthetic intermediate for the development of new pharmaceutical compounds. Its unique structure allows for the creation of novel molecules with potential therapeutic properties.
Used in Lipid Chemistry:
In the field of lipid chemistry, 2-O-Benzyl-3-O-allyl-sn-glycerol is used as a precursor for the synthesis of phospholipids or ether lipids. These lipids are essential components of cell membranes and have various biological functions, making them important targets for research and drug development.
Used in Cosmetics Industry:
2-O-Benzyl-3-O-allyl-sn-glycerol may also find applications in the cosmetics industry, where it can be used as a component in the formulation of skincare and hair care products. Its unique structure could potentially contribute to the development of innovative products with enhanced properties.
Used in Research and Development:
As a synthetic intermediate, 2-O-Benzyl-3-O-allyl-sn-glycerol is valuable in research and development for the creation of new compounds with potential applications in various fields, including pharmaceuticals, materials science, and biotechnology. Its versatility makes it a useful tool for scientists and researchers working on the development of novel molecules and materials.

Upstream product

• 1708-39-0 (S)-1,2-O-benzylideneglycerol 
• 909701-53-7 (R)-(2-phenyl-1,3-dioxolan-4-yl)methanol 
• 100-39-0 benzyl bromide 
• 71026-29-4 (S)-1-O-Trityl-3-O-allyl-glycerol 
• 173950-08-8 (S)-1-(allyloxy)-3-(bis(4-methoxyphenyl)(phenyl)methoxy)propan-2-ol 
• 56083-15-9 (S)-4-((allyloxy)methyl)-2,2-dimethyl-1,3-dioxolane 
• 123-34-2 (R)-3-allyloxypropane-1,2-diol 
• 117606-87-8 (S)-1-O-allyl-2,3-O-benzylideneglycerol 
• 117606-89-0 1-O-trityl-2-O-benzyl-3-O-allyl-sn-glycerol 
• 10160-05-1 (R)-1,2-O-benzylidene-3-O-hexadecylglycerol 

Downstream Products

• 92982-68-8 2-O-benzyl-3-O-(4-oxovaleryl)-sn-glycerol-<(1->3)-2,2,2-tribromoethylphospho>-2-O-benzyl-sn-glycerol-<(1->3)-chlorophenylphospho>-2,3-di-O-benzyl-sn-glycerol 
• 92982-69-9 2-O-benzyl-sn-glycerol-<(1->3)-2,2,2-tribromoethylphospho>-2-O-benzyl-sn-glycerol-<(1->3)-2-chlorophenylphospho>-1,2-di-O-benzyl-sn-glycerol 
• 92982-65-5 2-O-benzyl-3-O-(4-oxovaleryl)-sn-glycer-1-yl 2-O-benzyl-O-(1-propenyl)-sn-glycer-3-yl 2,2,2-tribromoethyl phosphate 
• 92982-67-7 2-O-benzyl-sn-glycer-3-yl 2-O-benzyl-3-O-(4-oxovaleryl)-sn-glycer-1-yl 2,2,2-tribromoethyl phosphate 
• 92982-66-6 2-O-benzyl-sn-glycer-1-yl 2-O-benzyl-1-O-(1-propenyl)-sn-glycer-3-yl 2,2,2-tribromoethyl phosphate 
• 92982-64-4 2-O-benzyl-3-O-(4-oxovaleryl)-sn-glycerol 
• 92982-62-2 2-O-benzyl-3-O-(4-oxovaleryl)-1-O-(1-propenyl)-sn-glycerol 
• 145398-52-3 1-O-myristoyl-2-O-benzyl-sn-glycerol 
• 91274-00-9 2-bromoethyl 2-O-benzyl-L-1-O-hexadecyl-glyceryl hydrogen phosphate 
• 84415-89-4 (S)-2-benzyloxy-3-hexadecyloxy-propan-1-ol 
• 130189-84-3 2-((R)-2-Benzyloxy-3-hexadecyloxy-propoxy)-[1,3,2]dioxaphospholane 2-oxide 
• 173950-09-9 Trifluoro-methanesulfonic acid (S)-3-allyloxy-2-benzyloxy-propyl ester 
• 92982-61-1 2-O-benzyl-1-O-(1-propenyl)-sn-glycerol 
• 92982-63-3 1-O-allyl-2-O-benzyl-3-O-(4-oxovaleryl)-sn-glycerol 

Relevant articles and documents

Synthesis of novel mimetics of the sialyl Lewis X determinant

Mimetics of the sialyl Lewis-X determinant in which at least one sugar domain is simulated by a di-, tri- or tetraalcohol unit have been synthesized. The inhibitory potency of these compounds for E- and P-selectin mediated cell adhesion has been evaluated in cell culture assays. The receptor binding affinity of the best of these mimetics was slightly higher than that of the natural oligosaccharide ligand sialyl Lewis X.

The Chemistry of L-Ascorbic and D-Isoascorbic Acids. 2. R and S Glyceraldehydes from a Common Intermediate

(R)- and (S)-glyceraldehyde and glycerol derivatives have been prepared from (2R,3S)-1,2-O-isopropylidenebutane-1,2,3,4-tetrol. (2R,3S)- and (2S,3S)-1,2-O-benzylidenebutane-1,2,3,4-tetrol have been prepared and cleaved to give (R)- and (S)-1,2-O-benzylideneglyceraldehydes and -glycerols.The conservation of chirality and conversion to PAF analogues are also demonstrated.